A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583181



Internal ID20956252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112844530..112845862hg38UCSC Ensembl
chr10:114604289..114605621hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv888n223
Supporting Variantsnssv18221296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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